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Progress in Molecular and Subcellular Biology|November 2, 2006
Altered splicing in prelamin A-associated premature aging phenotypesAnnachiara De Sandre-Giovannoli, Nicolas Lévy
Human Molecular Genetics|September 22, 2006
Molecular bases of progeroid syndromesClaire L Navarro, Pierre Cau, Nicolas Lévy
Medecine Sciences : M/S|October 28, 2008
[A-type lamins and progeroïd syndromes : persistent farnesylation with dramatic effects]Claire L Navarro, Yannick Poitelon, Nicolas Lévy
Molecular Medicine (Cambridge, Mass.)|May 11, 2011
Translational research and therapeutic perspectives in dysferlinopathiesFlorian Barthélémy, Nicolas Wein, Martin Krahn, et al.
Genetic Testing and Molecular Biomarkers|November 26, 2009
Exclusion of mutations in the dysferlin alternative exons 1 of DYSF-v1, 5a, and 40a in a cohort of 26 patientsMartin Krahn, Véronique Labelle, Ana Borges, et al.
Neuromolecular Medicine|June 16, 2006
Molecular genetics of autosomal-recessive axonal Charcot-Marie-Tooth neuropathiesRafaëlle Bernard, Annachiara De Sandre-Giovannoli, Valérie Delague, et al.
Cells|November 8, 2024
Voltage-Gated Ion Channel Compensatory Effect in DEE: Implications for Future TherapiesKhadijeh Shabani, Johannes Krupp, Emilie Lemesre, et al.
Methods in Molecular Biology (Clifton, N.J.)|September 2, 2018
Dysferlin Exon 32 Skipping in Patient CellsFlorian Barthélémy, Sébastien Courrier, Nicolas Lévy, et al.
Journal of Neuromuscular Diseases|February 27, 2018
Muscle Cells Fix Breaches by Orchestrating a Membrane Repair BalletFlorian Barthélémy, Aurélia Defour, Nicolas Lévy, et al.
Methods (San Diego, Calif.)|April 13, 2020
Hutchinson-Gilford progeria syndrome: Rejuvenating old drugs to fight accelerated ageingSolenn M Guilbert, Déborah Cardoso, Nicolas Lévy, et al.
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